The etiology of cardiac hypertrophy in infants

• Published in: Scientific reports Vol. 11; no. 1; p. 10626
• Main Authors: Stegeman, Raymond, Paauw, Nina D., de Graaf, Rosalie, van Loon, Rosa L. E., Termote, Jacqueline U. M., Breur, Johannes M. P. J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 19.05.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 692/308; 692/308/3187; 692/4019; 692/699/75; Cardiovascular diseases; Congenital diseases; Coronary artery disease; Diabetes; Diabetes mellitus; Echocardiography; Etiology; Heart diseases; Humanities and Social Sciences; Hypertension; Hypertrophy; Infants; Insulin; Insulin resistance; multidisciplinary; Neuromuscular diseases; Prognosis; Science; Science (multidisciplinary); Septum; Ventricle
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-90128-3

This study aimed to describe the variety of etiologies currently identified in infants with cardiac hypertrophy (CH) and investigate whether there is a relation with hyperinsulinism, echocardiographic characteristics and prognosis. This retrospective cohort study included infants born between 2005 and 2018 with CH measured by echocardiography [interventricular septum (IVS) and/or left ventricular posterior wall (LVPW) thickness with Z -score ≥ 2.0]. Children with congenital heart disease or hypertension were excluded. Underlying diagnosis, echocardiographic and follow-up data were extracted from patient files. Seventy-one infants with CH were included. An underlying cause of CH was identified in two-thirds (n = 47). Most common etiologies of CH were malformation syndromes (n = 23, including Noonan n = 12) and maternal diabetes mellitus (n = 13). Less common causes were congenital hyperinsulinism (n = 3), metabolic- (n = 5), sarcomeric- (n = 2) and neuromuscular disease (n = 1). In half of the identified causes (n = 22) an association with hyperinsulinism was described, including maternal diabetes mellitus (n = 13), malformation syndromes with insulin resistance (n = 6) and congenital hyperinsulinism (n = 3). CH associated with hyperinsulinism was echocardiographically characterized by lower LVPW thickness, higher IVS:LVPW ratio and more frequent sole involvement of the IVS (all, p  ≤ 0.02). CH associated with hyperinsulinism normalized more often (41 vs. 0%) with lower mortality rates (14 vs. 44%) compared to CH not associated with hyperinsulinism (all, p  ≤ 0.03). Nowadays, an etiology of CH can be identified in the majority of infants. The development of CH is often associated with hyperinsulinism which is mainly characterized by focal hypertrophy of the IVS on echocardiography. Prognosis depends on the underlying cause and is more favorable in CH associated with hyperinsulinism.